Canonical Allele Identifier: CA1828287657
Gene: KCNV2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2717858_2717869delinsAGGCCAGCATCC , CM000671.2:g.2717858_2717869delinsAGGCCAGCATCC GRCh38
NC_000009.11:g.2717858_2717869delinsAGGCCAGCATCC , CM000671.1:g.2717858_2717869delinsAGGCCAGCATCC GRCh37
NC_000009.10:g.2707858_2707869delinsAGGCCAGCATCC NCBI36
NG_012181.1:g.5333_5344delinsAGGCCAGCATCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000382082.4:c.119_130delinsAGGCCAGCATCC MANE Select ENSP00000371514.3:p.Gln40=
ENST00000382082.3:c.119_130delinsAGGCCAGCATCC ENSP00000371514.3:p.Gln40=
NM_133497.3:c.119_130delinsAGGCCAGCATCC NP_598004.1:p.Gln40=
XR_929202.1:n.620_631delinsAGGCCAGCATCC
XR_929203.1:n.620_631delinsAGGCCAGCATCC
NM_133497.4:c.119_130delinsAGGCCAGCATCC MANE Select NP_598004.1:p.Gln40=